Director, Medical and Scientific Affairs, General Medicine

Clario

7d•Hybrid

About The Position

At Clario, we transform lives by unlocking better evidence. As Director of Medical and Scientific Affairs, you will play a pivotal role in advancing clinical science and supporting our global operations. This position drives innovation in imaging solutions, strengthens client partnerships, and ensures excellence in trial delivery. Join us to make a meaningful impact on patient outcomes worldwide. At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster. Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.

Requirements

MD or PhD in a scientific discipline
5+ years of experience in medical imaging and clinical trials within CRO or pharma
Expertise in respiratory imaging, rare diseases, or pediatric conditions using MR, CT, X-ray, or Ultrasound
Strong knowledge of GCP, ICH guidelines, and FDA regulations
Proven ability in project planning, reporting, and financial management
Excellent communication, presentation, and organizational skills
Proficiency with office software (Word, Excel, PowerPoint, Outlook)
Ability to travel up to 30% and work in a hybrid environment

Responsibilities

Partner with Business Development to secure new opportunities and expand market share
Advise clients on imaging strategies and ensure successful trial execution
Provide medical and scientific expertise to internal teams for project delivery
Review and edit clinical trial protocols, imaging manuals, and study documentation
Lead governance meetings and represent Clario at Investigator Meetings
Train study teams and mentor staff on imaging and scientific requirements
Monitor reader performance and participate in Read Monitoring Board activities
Drive process improvements and technology enhancements for imaging services
Collaborate with product development and cross-functional teams on system requirements
Support proposal development and client presentations for new business opportunities